Canonical Allele Identifier: PA2827998634
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asp2431Asn
CA013697
NM_001354901.2:c.7291G>A